5-Bromo-2-methoxyaniline, 97%, Thermo Scientific Chemicals
5-Bromo-2-methoxyaniline, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

5-Bromo-2-methoxyaniline, 97%, Thermo Scientific Chemicals

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Quantity:
25 g
5 g
Catalog number B25693.14
also known as B25693-14
Price (USD)/ Each
394.00
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Quantity:
25 g
Request bulk or custom format
Price (USD)/ Each
394.00
Add to cart
5-Bromo-2-methoxyaniline, 97%, Thermo Scientific Chemicals
Catalog numberB25693.14
Price (USD)/ Each
394.00
-
Add to cart
Chemical Identifiers
CAS6358-77-6
IUPAC Name5-bromo-2-methoxyaniline
Molecular FormulaC7H8BrNO
InChI KeyOPGNSNDTPPIYPG-UHFFFAOYSA-N
SMILESCOC1=C(N)C=C(Br)C=C1
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to cream to pale brown or pale grey
FormCrystals or powder or crystalline powder
Assay (GC)≥96.0%
Melting Point (clear melt)92.5-101.5?C
5-Bromo-2-methoxyaniline is used as a pharmaceutical intermediate.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
5-Bromo-2-methoxyaniline is used as a pharmaceutical intermediate.

Solubility
Slightly soluble in water.

Notes
Preserve in well- closed, light- resistant & tight container. Store in cool & dry place.
RUO – Research Use Only

General References:

  1. F. Bergmann, David Schapiro. Applications of the meerwein reaction. part iv. the synthesis of new mono- and di-substituted stilbenes. J. Org. Chem. 1947, 12 (1), 57-66.
  2. Yoshiaki Kitamura; Ai Sakurai; Takahiro Udzu; Tomohiro Maegawa; Yasunari Monguchi; Hironao Sajiki. Heterogeneous Pd/C-catalyzed ligand-free Suzuki-Miyaura coupling reaction using aryl boronic esters. Tetrahedron. 2007, 63 (43), 10596-10602.